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Bioinformatics (Oxford, England)|May 10, 2007
Madeline 2.0 PDE: a new program for local and web-based pedigree drawingEdward H Trager, Ritu Khanna, Adrian Marrs, et al.JAMA Ophthalmology|February 22, 2019
Evaluation of an Algorithm for Identifying Ocular Conditions in Electronic Health Record DataJoshua D Stein, Moshiur Rahman, Chris Andrews, et al.American Journal of Medical Genetics. Part A|September 24, 2004
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10Satoko Shimizu, Charles Krafchak, Nobuo Fuse, et al.American Journal of Human Genetics|February 18, 2004
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage diseaseGonçalo R Abecasis, Beverly M Yashar, Yu Zhao, et al.American Journal of Human Genetics|October 28, 2005
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.American Journal of Human Genetics|June 13, 2009
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosaJames S Friedman, Joseph W Ray, Naushin Waseem, et al.Plos Genetics|May 10, 2012
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucomaJaney L Wiggs, Brian L Yaspan, Michael A Hauser, et al.Pageof 1